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四硫杂富瓦烯-D4 | 51751-16-7

中文名称
四硫杂富瓦烯-D4
中文别名
——
英文名称
tetrathiafulvalene-d4
英文别名
Tetrathiafulvalen-d4;Tetrathiofulven-d4;Tetrathiofulvalen-d4;tetradeuterio-[2,2']bi[1,3]dithiolylidene;4,5-dideuterio-2-(4,5-dideuterio-1,3-dithiol-2-ylidene)-1,3-dithiole
四硫杂富瓦烯-D4化学式
CAS
51751-16-7
化学式
C6H4S4
mdl
——
分子量
208.33
InChiKey
FHCPAXDKURNIOZ-RHQRLBAQSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    117.0 to 121.0 °C

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    101
  • 氢给体数:
    0
  • 氢受体数:
    4

SDS

SDS:7acf5f835668ef41bbd4d6103119d9b2
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反应信息

  • 作为产物:
    描述:
    tetrakis(trimethylsilyl)tetrathiafulvalene 在 乙醇-D1重水potassium carbonatepotassium hydrogencarbonate 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 以95%的产率得到四硫杂富瓦烯-D4
    参考文献:
    名称:
    Synthesis and reactivities of trimethylsilyl-substituted tetrathia- and tetraselenafulvalenes
    摘要:
    DOI:
    10.1021/jo00215a041
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文献信息

  • OKAMOTO, YOSHIYUKI;LEE, HUNG, SUI;ATTARWALA, S. T., J. ORG. CHEM., 1985, 50, N 15, 2788-2790
    作者:OKAMOTO, YOSHIYUKI、LEE, HUNG, SUI、ATTARWALA, S. T.
    DOI:——
    日期:——
  • BARRIERS AND FILMS
    申请人:Iwamoto Takashi
    公开号:US20130091803A1
    公开(公告)日:2013-04-18
    Provided herein are various bathers and methods of making and using them. In some embodiments, the barriers include a porous crystalline charge-transfer complex and a filler.
  • US9260574B2
    申请人:——
    公开号:US9260574B2
    公开(公告)日:2016-02-16
  • [EN] BARRIERS AND FILMS<br/>[FR] BARRIÈRES ET FILMS
    申请人:EMPIRE TECHNOLOGY DEV LLC
    公开号:WO2013058744A1
    公开(公告)日:2013-04-25
    Resin composites (10), which may be used as oxygen barrier films for preserving foods, include oxygen-resistant fillers (41), being filler materials (40) coated with porous crystalline charge-transfer complexes (CTCs) (20), that inhibit the passage of foreign molecules such as water or oxygen (30) through the film from an external side (50) to an internal side (60) by increasing the path (35) by which the molecules must travel. The composites may contain other resin or polymer components (25). The fillers may be flaked, oxygen-resistant fillers such as montmorillonite, bentonite, smectite, or artificial smectite. The CTCs may be derived from an organic acceptor such as tetracyanquinodimethane (TCNQ), trichloroethylene (TCE), and/or bis dithiobenzyl nickel; an organic electron donor such as bipyridine, pyridine, quinoline, isoquinoline, or tetrathiafulvalene (TTF); and a metal ion such as zinc, copper, iron, or nickel.
  • Synthesis and reactivities of trimethylsilyl-substituted tetrathia- and tetraselenafulvalenes
    作者:Yoshiyuki Okamoto、Hung Sui Lee、S. T. Attarwala
    DOI:10.1021/jo00215a041
    日期:1985.7
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同类化合物

四硫杂富瓦烯-D4 四硫富瓦烯 四(戊硫代)四硫富瓦烯 四(十八烷基硫代)四硫富瓦烯 四(乙硫基)四硫富瓦烯[有机电子材料] 双(亚乙基二硫醇)四硫代富瓦烯 双(三亚甲基二硫代)四硫富瓦烯 [1,3]二噻唑并[4,5-d]-1,3-二噻唑,2,5-二(1,3-二硫醇-2-亚基)- 5-甲基二硫杂环戊烯-3-硫酮 5-氨基-3-硫代氧基-3H-(1,2)二硫杂环戊烯-4-羧酸乙酯 5-氨基-3-硫代氧基-3H-(1,2)二硫杂环戊烯-4-甲腈 5,6-二氢-4H-环戊并[1,2]二硫代-3-硫酮 4,4’,5-三甲基四硫富瓦烯 4-甲基二硫杂环戊烯-3-硫酮 4-新戊基-3H-1,2-二硫杂环戊烯-3-硫酮 4,5-二甲基-3H-1,2-二硫醇-3-酮 4,5,6,7-四氢苯并[1,2]二硫-3-硫酮 4,4’-二甲基连四硫富瓦烯 4,4,5,5,6,6,7,7-八氢二苯并四硫富瓦烯 3H-1,2-二硫杂环戊二烯-3-酮 3H-1,2-二硫杂环戊二烯-3-硫酮 2-(4,5-二甲基-1,3-二硫杂环戊烯-2-亚基)-4,5-二甲基-1,3-二硫杂环戊烯 2,3,6,7-四(2-氰乙基硫代)四硫富瓦烯 1,3-二噻唑,2-[4,5-二(癸基硫代)-1,3-二硫醇-2-亚基]-4,5-二(癸基硫代)- (四甲基硫)四硫富瓦烯 2,3,6,7-tetrakis[2-(2-methoxyethoxy)ethylsulfanyl]tetrathiafulvalene 2,3-bis[2-(2-methoxyethoxy)ethylsulfanyl]-6,7-bis(methylsulfanyl)tetrathiafulvalene (5S,6S,5'S,6'S)-5,5',6,6'-tetramethyl-bis(ethylenedithio)tetrathiafulvalene 2,5-bis(4,5-ethylenedithio-1,3-dithiol-2-ylidene)-1,3,4,6-tetrathiapentalene 2,3,6,7-Tetrakis(1-octyloxymethyl)tetrathiafulvalene 2,3,6,7-Tetrakis(1-dodecyloxymethyl)tetrathiafulvalene 2,3,6,7-Tetrakis(1-pentyloxymethyl)tetrathiafulvalene 2,3,6,7-Tetrakis(1-hexyloxymethyl)tetrathiafulvalene 2,3,6,7-Tetrakis(1-propoxymethyl)tetrathiafulvalene 2,3,6,7-Tetrakis(1-decyloxymethyl)tetrathiafulvalene 2,3,6,7-Tetrakis(1-heptyloxymethyl)tetrathiafulvalene 2,6-bis(thioacetopentadecylamido)-3,7-bis(methylthiotetrathiafulvalene) 2,7-bis(thioacetopentadecylamido)-3,6-bis(methylthiotetrathiafulvalene) ethane 1,2-dithiol 2,3,6,7-Tetrakis(1-tetradecyloxymethyl)tetrathiafulvalene 2-Isopropyliden-1,3-dithiol-4,5-dicarbonitril 4,5-bis(butylthio)tetrathiafulvalene 2,3-dicyano-6,7-bis(butylthio)tetrathiafulvalene Tetrabutylammonium-(3-thioxo-3H-1,2-dithiol-5-thiolat) 5,6-dihydro-5-dimethoxymethyl-2-(5',6'-dihydro-1,3-dithiolo[4,5-b]-1,4-dithiin-2'-ylidene)-1,3-dithiolo[4,5-b]-1,4-dithiin 3H-1,2-dithiole 2,2'-(But-2-en-1,4-diyliden)bis[1,3-dithiol-4,5-dicarbonitril] 3-methylsulfanyl-[1,2]dithiolylium; iodide 2,2'-(Dodeca-2,4,6,8,10-pentaen-1,12-diyliden)bis[1,3-dithiol-4,5-dicarbonitril] (E,E)-1,6-bis[4,5-bis(methylsulfanyl)-1,3-dithiol-2-ylidene]hexa-2,4-diene